Immunogenicity and Protective Efficacy of Radiation-Attenuated and Chemo-Attenuated PfSPZ Vaccines in Equatoguinean Adults
Plasmodium falciparum sporozoite (PfSPZ) Vaccine (radiation-attenuated, aseptic, purified, cryopreserved PfSPZ) and PfSPZ-CVac (infectious, aseptic, purified, cryopreserved PfSPZ administered to subjects taking weekly chloroquine chemoprophylaxis) have shown vaccine efficacies (VEs) of 100% against...
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Published in | The American journal of tropical medicine and hygiene Vol. 104; no. 1; pp. 283 - 293 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Institute of Tropical Medicine
01.01.2021
The American Society of Tropical Medicine and Hygiene |
Subjects | |
Online Access | Get full text |
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Summary: | Plasmodium falciparum
sporozoite (PfSPZ) Vaccine (radiation-attenuated, aseptic, purified, cryopreserved PfSPZ) and PfSPZ-CVac (infectious, aseptic, purified, cryopreserved PfSPZ administered to subjects taking weekly chloroquine chemoprophylaxis) have shown vaccine efficacies (VEs) of 100% against homologous controlled human malaria infection (CHMI) in nonimmune adults.
Plasmodium falciparum
sporozoite-CVac has never been assessed against CHMI in African vaccinees. We assessed the safety, immunogenicity, and VE against homologous CHMI of three doses of 2.7 × 10
6
PfSPZ of PfSPZ Vaccine at 8-week intervals and three doses of 1.0 × 10
5
PfSPZ of PfSPZ-CVac at 4-week intervals with each arm randomized, double-blind, placebo-controlled, and conducted in parallel. There were no differences in solicited adverse events between vaccinees and normal saline controls, or between PfSPZ Vaccine and PfSPZ-CVac recipients during the 6 days after administration of investigational product. However, from days 7–13, PfSPZ-CVac recipients had significantly more AEs, probably because of Pf parasitemia. Antibody responses were 2.9 times higher in PfSPZ Vaccine recipients than PfSPZ-CVac recipients at time of CHMI. Vaccine efficacy at a median of 14 weeks after last PfSPZ-CVac dose was 55% (8 of 13,
P
= 0.051) and at a median of 15 weeks after last PfSPZ Vaccine dose was 27% (5 of 15,
P
= 0.32). The higher VE in PfSPZ-CVac recipients of 55% with a 27-fold lower dose was likely a result of later stage parasite maturation in the liver, leading to induction of cellular immunity against a greater quantity and broader array of antigens. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 ObjectType-Undefined-3 Financial support: This work supported was by a public–private partnership, the EGMVI, made up of the government of EG Ministries of Mines and Hydrocarbons, and Health and Social Welfare, Marathon EG Production Limited, Noble Energy, Atlantic Methanol Production Company, and EG LNG. Disclosures: Sanaria Inc. manufactured PfSPZ Vaccine and Protein Potential LLC is affiliated with Sanaria. Sanaria is the sponsor of the clinical trial. L. W. P. C., N. K. C., E. R. J., T. S., Y. A., T. M., P. F. B., B. K. L. S., T. L. R., and S. L. H. are salaried, full-time employees of Sanaria Inc., the developer and sponsor of Sanaria PfSPZ Vaccine. SRM and E.S. were a salaried, full-time employee of Sanaria Inc. at the time the trial was conducted. Thus, all authors associated with Sanaria or Protein Potential have potential conflicts of interest. Authors’ addresses: Said A. Jongo, Ally Olotu, Ali Mtoro, Ali Hamad, Elizabeth Nyakarungu, Mwajuma Chemba, Kamaka R. Kassim, and Salim Abdulla, Ifakara Health Institute, Bagamoyo Research and Training Centre, Bagamoyo, Tanzania, E-mails: sjongo@ihi.or.tz, aolotu@ihi.or.tz, amtoro@ihi.or.tz, ahamad@ihi.or.tz, enyakarungu@ihi.or.tz, mchemba@ihi.or.tz, kramadhani@ihi.or.tz, and sabdulla@ihi.or.tz. Vicente Urbano, José Raso Bijeri, Martin Eka Ondo Mangue, Beltrán Ekua Ntutumu Pasialo, Genaro Nsue Nguema, Salomon Nguema Owono, Matilde Riloha Rivas, and Mitoha Ondo’o Ayekaba, Ministry of Health and Social Welfare, Government of Equatorial Guinea, Malabo, Bioko Norte, Equatorial Guinea, E-mails: viceurb2013@gmail.com, jraso@mcd.org, mondo@mcd.org, bntutumu@mcd.org, gnguema@mcd.org, mitoha.ondo@gob.gq, mrriloha@gmail.com, and mitoha_ondo@yahoo.com. L. W. Preston Church, Eric R. James, Thomas C. Stabler, Yonas Abebe, Tooba Murshedkar, Peter F. Billingsley, Thomas L. Richie, and Stephen L. Hoffman, Sanaria Inc., Rockville, MD, E-mails: lwpchurch@sanaria.com, ejames@sanaria.com, tstabler@sanaria.com, yabebe@sanaria.com, tmurshedkar@sanaria.com, pbillingsley@sanaria.com, trichie@sanaria.com, and slhoffman@sanaria.com. Stephen R. Manock, Department of Family Medicine, John Peter Smith Hospital, Fort Worth, TX, E-mail: smanock@jpshealth.org. Tobias Schindler, Maximillian Mpina, Anna Deal, Julian Sax, Salome Hosch, Anneth Tumbo, Linda Gondwe, J. Luis Segura, Marcel Tanner, and Claudia Daubenberger, Swiss Tropical and Public Health Institute, Basel, Switzerland, E-mails: tobias.schindler@swisstph.ch, mmpina@ihi.or.tz, annacadeal@gmail.com, julian_sax@gmx.de, salome.hosch@swisstph.ch, atumbo@ihi.or.tz, 92lindageoffrey@gmail.com, ,luis.segura@swisstph.ch, marcel.tanner@swisstph.ch, and claudia.daubenberger@swisstph.ch. Natasha KC and B. Kim Lee Sim, Sanaria Inc. and Protein Potential LLC, Rockville, MD, E-mails: nkc@sanaria.com and ksim@protpot.com. Elizabeth Saverino, Viela Bio, Gaithersburg, MD, Email: elizabeth.saverino@gmail.com. Carlos Cortes, Wonder Philip Phiri, Guillermo A. García, and Christopher Schwabe, Medical Care Development International, Silver Spring, MD, E-mails: ccortes@mcd.org, wphiri@mcd.org, ggarcia@mcd.org, and cschwabe@mcd.org. Dianna Hergott, Department of Epidemiology, University of Washington, Seattle, WA, E-mail: dhergott@uw.edu. Carl D. Maas, Center for Child and Family Studies, College of Social Work, University of South Carolina, Columbia SC, E-mail: cdmaas@mailbox.sc.edu. |
ISSN: | 0002-9637 1476-1645 1476-1645 |
DOI: | 10.4269/ajtmh.20-0435 |